Canonical Allele Identifier: CA2652992722

Gene: ADA

Linked Data

• gnomAD v4: 20-44651955-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.44651955T>A , CM000682.2:g.44651955T>A	GRCh38
NC_000020.10:g.43280596T>A , CM000682.1:g.43280596T>A	GRCh37
NC_000020.9:g.42714010T>A	NCBI36
NG_007385.1:g.4781A>T , LRG_16:g.4781A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000536076.2:c.-174A>T	ENSP00000512234.1:n.-174A>T
ENST00000696039.1:n.268A>T
ENST00000696062.1:c.96+145A>T	ENSP00000512365.1:n.96+145A>T
ENST00000696064.1:c.-171A>T	ENSP00000512367.1:n.-171A>T
ENST00000535573.1:n.279A>T
ENST00000536076.1:n.160A>T
XM_011528479.1:c.-310A>T	XP_011526781.1:n.-310A>T